510(k) K800023 ยท CAF Nebulizer (Direct Patient Interface)
LUNG AEROSOL UNIT
| Applicant | Cadema Medical Products, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Jan 1, 1985 |
| Received | Jan 7, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K800023
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.